A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035135



Internal ID15888321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75521024..75535673hg38UCSC Ensembl
Innerchr5:74816849..74831498hg19UCSC Ensembl
Innerchr5:74852605..74867254hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3814650
hg1914650
hg1814650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598674
Supporting Variants
Samples
Known GenesPOLK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035135
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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